It looks like you're using an Ad Blocker.
Please white-list or disable AboveTopSecret.com in your ad-blocking tool.
Thank you.
Some features of ATS will be disabled while you continue to use an ad-blocker.
Controls involving placebos for unproven treatments are not unethical
Studies from the United States, the United Kingdom, Brazil, and Spain looked at whether hydroxychloroquine prevented people from getting infected with the coronavirus, or helped them recover faster.
All of the studies randomly assigned patients to treatment and control (non-treatment) groups.
None of the studies found that hydroxychloroquine made a difference.
I seem to remember the Remdesivir trial wasn't completed because it appeared those on the control placebo group would at a higher risk of dying.
The primary end point was additionally assessed by medication adherence, zinc use, or vitamin C use as post hoc analyses. The Supplement gives additional detail on statistical methods and sensitivity analyses.
I seem to remember the Remdesivir trial wasn't completed because it appeared those on the control placebo group would at a higher risk of dying
www.theguardian.com...
This article was amended on 30 April 2020. An earlier version said that the remdesivir trial had been stopped early because of side-effects. Although some patients were taken off the drug because of side-effects, it was stopped early because they did not recruit enough patients.
Behind that ray of hope, though, was one of the toughest quandaries in medicine: how to balance the need to rigorously test a new medicine for safety and effectiveness with the moral imperative to get patients a treatment that works as quickly as possible. At the heart of the decision about when to end the trial was a process that was — as is often in the case in clinical trials — by turns secretive and bureaucratic.
The National Institute of Allergy and Infectious Diseases has described to STAT in new detail how it made its fateful decision: to start giving remdesivir to patients who had been assigned to receive a placebo in the study, essentially limiting researchers’ ability to collect more data about whether the drug saves lives — something the study, called ACTT-1, suggests but does not prove. In the trial, 8% of the participants given remdesivir died, compared with 11.6% of the placebo group, a difference that was not statistically significant.
A top NIAID official said he had no regrets about the decision.
And none of those 5 trials mirrored the treatment proposed by front line doctors.
I seem to remember the Remdesivir trial wasn't completed because it appeared those on the control placebo group would at a higher risk of dying
When the remdesivir results were announced, the NIH said the data came from an “interim” analysis. This means that a study was stopped early because a drug’s benefit was so undeniable that it would be unethical to continue the study. But Lane said this was incorrect. The data come from a preliminary final analysis, a point at which the study would normally end.
Here's one that looked at your precious zinc.
did miss this phrase
a study was stopped early
has cost up to 100,000 American lives.